Non-alcoholic Fatty Liver Disease NAFLD, Non-alcoholic Steatohepatitis NASH
Conditions
Keywords
Empagliflozin, Statin, Pioglitazone, NAFLD, NASH
Brief summary
The goal of this clinical trial is to assess the efficacy of Empagliflozin versus Statins as monotherapy and polytherapy in non-alcoholic fatty liver disease and non-alcoholic Steatohepatitis. Does drug ABC Empagliflozin versus Statins as monotherapy and polytherapy improve the controlled attenuation parameter (CAP), the liver stiffness measurement (LSM), the proportion of patients with at least one point improvement or one-stage reduction in the histological scores with respect to hepatic steatosis, hepatocellular ballooning, lobular inflammation, and fibrosis after treatment? What medical problems do participants have when taking Empagliflozin versus Statins as monotherapy and polytherapy? Participants will: * Take Empagliflozin alone or Empagliflozin plus statins or Pioglitazone plus Statins or Pioglitazone alone as standard therapy every day for 3 months * Be directed to complete history taking. FibroScan®, abdominal ultrasound and laboratory tests of ALT, AST, ALP, platelets count, Triglycerides, Cholesterol, LDL, HDL, serum insulin and insulin resistance will be conducted at baseline and after the drug administration for 3 months. * Keep a diary of recording any side effects they use a rescue inhaler
Detailed description
NAFLD is a growing global health problem linked with metabolic issues like obesity, diabetes, and insulin resistance. It ranges from simple liver fat accumulation to NASH, involving inflammation and liver damage, progressing to fibrosis, cirrhosis, and cancer. Managing NAFLD is tough due to diagnosis challenges and metabolic complications. Lifestyle changes like diet and exercise are key but often hard to sustain. No FDA-approved treatments exist yet, but drugs like Empagliflozin and statins are being studied for their potential to improve insulin sensitivity, reduce liver inflammation, and slow disease progression. This study compares these therapies for NAFLD and NASH.
Interventions
30 mg orally once daily
10 mg orally once daily
20 mg orally once daily
Orally once daily of each (10 mg, 20 mg respectively)
Orally once daily of each (30mg and 20mg respectively)
Sponsors
Study design
Eligibility
Inclusion criteria
* Adult * Obese * Hyperlipidemic * Diabetic patients * Diagnosed with non-alcoholic fatty liver disease and non-alcoholic Steatohepatitis
Exclusion criteria
* Pregnant women * Breast feeding women * Diabetic patients with ketoacidosis * Hyperlipidemic patients with cardiovascular dysfunction * Patients with NAFLD or NASH induced hepatocellular carcinoma * Hyperlipidemic obese diabetic patients diagnosed with NAFLD or NASH who will refuse to sign the informed consent
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The controlled attenuation parameter (CAP). | After 3 months | The CAP value is expressed in dB/m. |
| The liver stiffness measurement (LSM) using FibroScan®. | After 3 months | The LSM value is expressed as kilopascal or kPa. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Fibrosis-4 (FIB-4) index | After 3 months | FIB-4 is a non-invasive scoring system that can predict significant hepatic fibrosis patients. |
Countries
Egypt